Positron Emission Tomography with Pittsburgh Compound B in Diagnosis of Early Stage Alzheimer’s Disease

被引:0
作者
Jianjun Jia
Binbin Sun
Zhe Guo
Jinming Zhang
Jiahe Tian
Hongchuan Tang
Luning Wang
机构
[1] PLA General Hospital,Department of Geriatric Neurology
[2] Affiliated Hospital for Academy of Military Medical Sciences,Department of Neurology
[3] PLA General Hospital,Department of Nuclear Medicine
来源
Cell Biochemistry and Biophysics | 2011年 / 59卷
关键词
Alzheimer’s disease; Mild cognitive impairment; Positron emission tomography; Pittsburgh compound B; β-amyloid;
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学科分类号
摘要
In order to evaluate the role of positron emission tomography (PET) with N-methyl-[11C]-2-(4′-methylaminophenyl)-6-hydroxybenzothiazole, also known as Pittsburgh compound B (PIB), in the early diagnosis of Alzheimer’s disease (AD). Clinical data were collected, and PIB PET cerebral imaging was performed in patients with AD (n = 6), mild cognitive impairment (MCI) (n = 7), and elderly, mentally normal controls (NCs) (n = 7). PET images of the subjects were then analyzed. Visual analysis showed that the radioactivity clearance rate in AD patients was significantly different from that found in the NC group. Furthermore, the radioactivity clearance rate 45 min after PIB injection was significantly lower than the NC group. Images from the MCI group presented heterogeneous results, overlapping with those from both the AD and NC groups. Statistical analysis showed that the radioactivity clearance rate during 5–45 min post-injection was significantly lower in the AD group (41–77%) than the control group (75–81%) (P > 0.05) and the MCI group (59–77%). The radioactivity clearance rate in the bilateral parietal lobes, frontal, temporal, and right occipital lobes, and the bilateral corpora striata in MCI group were lower than that in control group (P < 0.05). PIB PET brain imaging can differentiate early AD patients from NCs and may have certain value in identifying patients progressing to MCI.
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页码:57 / 62
页数:5
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  • [11] Steffens DC(2007)Research criteria for the diagnosis of Alzheimer’s disease: revising the NINCDS–ADRDA criteria Lancet Neurology 6 734-368
  • [12] Willis RJ(1999)Tangles and plaques in nondemented aging and “preclinical” Alzheimer’s disease Annals of Neurology 45 358-355
  • [13] Wallace RB(2003)Prognostic value of regional cerebral metabolism in patients undergoing dementia evaluation: comparison to a quantifying parameter of subsequent cognitive performance and to prognostic assessment without PET Molecular Genetics and Metabolism 80 350-157
  • [14] Hardy JA(2007)The utility of PET brain imaging in the initial evaluation of dementia Journal of the American Medical Directors Association 8 150-508
  • [15] Higgins GA(2007)Amyloid, hypometabolism, and cognition in Alzheimer disease: an [11C]PIB and [18F]FDG PET study Neurology 68 501-2754
  • [16] Mirra SS(2003)Synthesis and evaluation of 11C-labeled 6-substituted 2-arylbenzothiazoles as amyloid imaging agents Journal of Medicinal Chemistry 46 2740-112
  • [17] Heyman A(2009)Cortical PIB binding in Lewy body disease is associated with Alzheimer-like characteristics Neurobiology of Diseases 34 107-1212
  • [18] McKeel D(2007)11C-PIB PET imaging in Alzheimer disease and frontotemporal lobar degeneration Neurology 68 1205-2615
  • [19] Sumi SM(2007)PIB is a non-specific imaging marker of amyloid-beta (Abeta) peptide-related cerebral amyloidosis Brain 130 2607-undefined
  • [20] Crain BJ(undefined)undefined undefined undefined undefined-undefined